Federico Zara

25.1k total citations
242 papers, 6.6k citations indexed

About

Federico Zara is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Federico Zara has authored 242 papers receiving a total of 6.6k indexed citations (citations by other indexed papers that have themselves been cited), including 105 papers in Molecular Biology, 94 papers in Genetics and 63 papers in Psychiatry and Mental health. Recurrent topics in Federico Zara's work include Genetics and Neurodevelopmental Disorders (70 papers), Epilepsy research and treatment (60 papers) and Glycogen Storage Diseases and Myoclonus (41 papers). Federico Zara is often cited by papers focused on Genetics and Neurodevelopmental Disorders (70 papers), Epilepsy research and treatment (60 papers) and Glycogen Storage Diseases and Myoclonus (41 papers). Federico Zara collaborates with scholars based in Italy, United States and United Kingdom. Federico Zara's co-authors include Pasquale Striano, Carlo Minetti, Salvatore Striano, Claudio Bruno, Elena Di Gennaro, F. Dagna Bricarelli, Ingrid E. Scheffer, Michael P. Lisanti, Federica Sotgia and Fabio Benfenati and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Federico Zara

230 papers receiving 6.5k citations

Peers

Countries citing papers authored by Federico Zara

Since Specialization

Citations

This map shows the geographic impact of Federico Zara's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Federico Zara with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Federico Zara more than expected).

Fields of papers citing papers by Federico Zara

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Federico Zara. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Federico Zara. The network helps show where Federico Zara may publish in the future.

Co-authorship network of co-authors of Federico Zara

This figure shows the co-authorship network connecting the top 25 collaborators of Federico Zara. A scholar is included among the top collaborators of Federico Zara based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Federico Zara. Federico Zara is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Derivation of the IGGi006-A stem cell line from a patient with CAPRIN1 haploinsufficiency 2025 ·Stem Cell Research ·Giuseppina Conteduca, Chiara Baldo, (unknown), (unknown), Renata Bocciardi, (unknown), Sımona Baldassari, Maria Margherita Mancardi, Federico Zara, Michela Malacarne, Domenico Coviello	1
2	SLC35A2-Related Brain Disorders: Genetics, Pathophysiology, and Therapeutic Insights 2025 ·International Journal of Molecular Sciences ·(unknown), Antonella Riva, Greta Volpedo, Valerio Conti, (unknown), Federico Zara, (unknown), Antonio Falace	0
3	Medication‐resistant epilepsy is associated with a unique gut microbiota signature 2025 ·Epilepsia ·Antonella Riva, (unknown), Greta Volpedo, (unknown), (unknown), Valentina Biagioli, Ganna Balagura, Elisabetta Amadori, Carmen De, Emanuele Cerulli Irelli, Carlo Di Bonaventura, Federico Zara, Osman Uğur Sezerman, Emilio Russo, Pasquale Striano	3
4	A hypomorphic FLVCR2 variant resulting in moderate transport deficiency causes hydranencephaly syndrome with brain calcifications 2025 ·European Journal of Human Genetics ·Marcello Scala, (unknown), (unknown), Yu Zhang, (unknown), Mariasavina Severino, Francesca Madia, (unknown), (unknown), Valeria Capra, D. Paladini, (unknown), Ezio Fulcheri, (unknown), (unknown), Renata Bocciardi, Federico Zara, Long N. Nguyen	1
5	A claudin5-binding peptide enhances the permeability of the blood-brain barrier in vitro 2025 ·Science Advances ·(unknown), (unknown), Giulio Alberini, (unknown), (unknown), (unknown), Enrico Millo, (unknown), Clarissa Braccia, Andrea Armirotti, Francesco Pisani, Federico Zara, Valentina Castagnola, Luca Maragliano, Fabio Benfenati	4
6	Expanding the phenotype of UPF3B‐related disorder: Case reports and literature review 2024 ·American Journal of Medical Genetics Part A ·(unknown), Maria K. Haanpää, (unknown), (unknown), John R. Pollard, (unknown), Monica Traverso, Mariasavina Severino, (unknown), (unknown), Federico Zara, Francesca Faravelli, Valeria Capra, Marcello Scala	3
7	Overexpression of H2AFX gene in neuroblastoma is associated with worse prognosis 2024 ·Pediatric Blood & Cancer ·Marzia Ognibene, Stefano Parodi, Loredana Amoroso, Federico Zara, Annalisa Pezzolo	1
8	Validation of analytical methods for the production of expanded γδ T lymphocytes useful for therapeutic purposes 2024 ·Current Research in Translational Medicine ·Fabio Morandi, (unknown), Federico Zara, Irma Airoldi	0
9	DAG1 haploinsufficiency is associated with sporadic and familial isolated or pauci-symptomatic hyperCKemia 2024 ·European Journal of Human Genetics ·Monica Traverso, (unknown), Michele Iacomino, Marco Di Duca, Chiara Panicucci, (unknown), Marina Grandis, Antonio Falace, Annalaura Torella, Esther Picillo, (unknown), Luisa Politano, Vincenzo Nigro, A. Micheil Innes, Rita Barresi, Claudio Bruno, Federico Zara, Chiara Fiorillo, Marcello Scala	1
10	Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansions 2023 ·Epilepsia ·Mark Corbett, Christel Depienne, Liana Veneziano, Karl Martin Klein, Francesco Brancati, Renzo Guerrini, Federico Zara, Shoji Tsuji, Jozef Gécz	11
11	Novel SYNGAP1 Variant in an Adult Individual Affected by Intellectual Disability and Epilepsy: A Cold Case Solved through Whole-Exome Sequencing 2023 ·Molecular Syndromology ·(unknown), (unknown), Maria Teresa Divizia, Livia Pisciotta, Maria Margherita Mancardi, Margherita Lerone, (unknown), (unknown), (unknown), Diego Vozzi, (unknown), Stefano Gustincich, Lino Nobili, Federico Zara, Aldamaria Puliti	0
12	ATP12A Proton Pump as an Emerging Therapeutic Target in Cystic Fibrosis and Other Respiratory Diseases 2023 ·Biomolecules ·(unknown), (unknown), (unknown), (unknown), Federico Zara, Paolo Scudieri	1
13	Exome sequencing data screening to identify undiagnosed Aromatic l-amino acid decarboxylase deficiency in neurodevelopmental disorders 2023 ·Biochemical and Biophysical Research Communications ·Antonella Riva, Michele Iacomino, Chiara Piccardo, (unknown), (unknown), (unknown), Carlo Minetti, (unknown), Federico Zara, Marcello Scala, Pasquale Striano, Mariarita Bertoldi	5
14	Somatic Double Inactivation of NF1 Associated with NF1-Related Pectus Excavatum Deformity 2023 ·Human Mutation ·(unknown), Marcello Scala, Patrizia De Marco, (unknown), Marzia Ognibene, Francesca Madia, (unknown), Marco Di Duca, Michele Torre, (unknown), Paolo Scudieri, Gianluca Piccolo, Girolamo Mattioli, (unknown), Paolo Uva, Diego Vozzi, Ezio Fulcheri, Pasquale Striano, (unknown), Federico Zara	3
15	Vesicular Glutamate Release from Feeder-FreehiPSC-Derived Neurons 2022 ·International Journal of Molecular Sciences ·Sımona Baldassari, Chiara Cervetto, (unknown), Floriana Fruscione, Ganna Balagura, Simone Pelassa, Ilaria Musante, Michele Iacomino, Monica Traverso, Anna Corradi, Paolo Scudieri, Guido Maura, Manuela Marcoli, Federico Zara	8
16	The L467F-F508del Complex Allele Hampers Pharmacological Rescue of Mutant CFTR by Elexacaftor/Tezacaftor/Ivacaftor in Cystic Fibrosis Patients: The Value of the Ex Vivo Nasal Epithelial Model to Address Non-Responders to CFTR-Modulating Drugs 2022 ·International Journal of Molecular Sciences ·Elvira Sondo, Federico Cresta, (unknown), Valeria Tomati, Valeria Capurro, Emanuela Pesce, (unknown), Michele Iacomino, (unknown), Domenico Coviello, Tiziano Bandiera, Federico Zara, Luis J. V. Galietta, Renata Bocciardi, Carlo Castellani, Nicoletta Pedemonte	31
17	SLC26A9 as a Potential Modifier and Therapeutic Target in Cystic Fibrosis Lung Disease 2022 ·Biomolecules ·(unknown), Federico Zara, Paolo Scudieri	6
18	New phenotype caused by POMGNT2 mutations 2021 ·BMJ Case Reports ·(unknown), Chiara Fiorillo, Federico Zara, (unknown)	1
19	STXBP1 Syndrome Is Characterized by Inhibition-Dominated Dynamics of Resting-State EEG 2021 ·Frontiers in Physiology ·Simon J. Houtman, Hanna C. A. Lammertse, (unknown), Ganna Balagura, Elena Gardella, Jennifer R. Ramautar, (unknown), Rikke S. Møller, Federico Zara, Pasquale Striano, (unknown), Mieke M. van Haelst, Marc Engelen, Titia L. van Zuijen, Huibert D. Mansvelder, Matthijs Verhage, Hilgo Bruining, Klaus Linkenkaer‐Hansen	24
20	Galloway–Mowat syndrome: An early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literature 2010 ·Seizure ·Marianna Pezzella, (unknown), Pierangelo Veggiotti, Alberto Bettinelli, (unknown), Federico Zara, Pasquale Striano, Carlo Minetti	17

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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